Canonical Allele Identifier: CA481920468

Gene: TBX5

Linked Data

• MyVariant Identifiers: chr12:g.114836402G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.114398597G>A , CM000674.2:g.114398597G>A	GRCh38
NC_000012.11:g.114836402G>A , CM000674.1:g.114836402G>A	GRCh37
NC_000012.10:g.113320785G>A	NCBI36
NG_007373.1:g.14846C>T , LRG_670:g.14846C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405440.7:c.486C>T MANE Select	ENSP00000384152.3:p.Asn162=
ENST00000310346.8:c.486C>T	ENSP00000309913.4:p.Asn162=
ENST00000349716.9:c.336C>T	ENSP00000337723.5:p.Asn112=
ENST00000405440.6:c.486C>T	ENSP00000384152.2:p.Asn162=
ENST00000526441.1:c.486C>T	ENSP00000433292.1:p.Asn162=
ENST00000552726.1:n.537C>T
NM_000192.3:c.486C>T , LRG_670t1:c.486C>T	NP_000183.2:p.Asn162=
NM_080717.2:c.336C>T	NP_542448.1:p.Asn112=
NM_181486.2:c.486C>T	NP_852259.1:p.Asn162=
XM_017019912.1:c.534C>T	XP_016875401.1:p.Asn178=
NM_080717.3:c.336C>T	NP_542448.1:p.Asn112=
NM_181486.4:c.486C>T MANE Select	NP_852259.1:p.Asn162=
NM_080717.4:c.336C>T	NP_542448.1:p.Asn112=